The following data is part of a premarket notification filed by Ditron Precision Ltd with the FDA for Dental Implants And Abutments.
| Device ID | K161497 | 
| 510k Number | K161497 | 
| Device Name: | Dental Implants And Abutments | 
| Classification | Implant, Endosseous, Root-form | 
| Applicant | Ditron Precision Ltd Haofe 2 St., P.O Box 5010 Netanya, IL 78150 | 
| Contact | Moshe Orlev | 
| Correspondent | Tali Hazan Talmed Ltd Ramot Naftali, M.P Upper Galillee Ramot Naftali, IL 13830000  | 
| Product Code | DZE | 
| CFR Regulation Number | 872.3640 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2016-06-01 | 
| Decision Date | 2016-10-28 | 
| Summary: | summary |